Kostovski Ognen, Jovanovikj Rubens, Kostovska Irena
University Clinic of Digestive Surgery, Ss. Cyril and Methodius University Faculty of Medicine, Skopje, Macedonia.
Department of Pathology, Ss. Cyril and Methodius University Faculty of Medicine, Skopje, Macedonia.
Turk J Surg. 2025 May 30;41(2):174-179. doi: 10.47717/turkjsurg.2025.6837.
One of the most prevalent cancers in the world is colorectal carcinoma (CRC). Aggressive cancer forms and a poor prognosis are linked to cancer stem cell (CSC) markers. The study aimed to determine whether the co-expression of the CSC markers CD133 and CD44 could predict an increased risk of metastasis in colorectal cancer.
Our study included 90 patients with CRC. All patients were divided into two subgroups: Metastatic CRC and non-metastatic CRC. Initially, tumor samples were examined using conventional histological techniques, and then immunohistochemical analysis with monoclonal antibodies against CD133 and CD44 markers was performed.
High co-expression of CD133 and CD44 was observed in 71.4% of patients with metastatic disease, compared to 37.9% in patients without distant metastases. Discordant expression of both markers was found in 8% of the subgroup with metastatic CRC and 13.4% of the subset without metastatic CRC. Statistical analyses showed a significant association of increased expression of CD133 and CD44 with the disease stage, T- category, and N- nodal status. With multiple regression analysis, the stage of disease was singled out as the factor with the greatest and statistically significant influence on the expression of CD133 (p<0.0001) and CD44 (p<0.0001).
Co-expression of CD133 and CD44 plays an essential role in predicting the metastatic form of CRC. Both stem cell markers can be implemented in standard pathohistological diagnostics and can be useful markers for pre-therapeutic oncology screening.
结直肠癌(CRC)是世界上最常见的癌症之一。侵袭性癌症形式和不良预后与癌症干细胞(CSC)标志物有关。本研究旨在确定CSC标志物CD133和CD44的共表达是否可预测结直肠癌转移风险增加。
我们的研究纳入了90例CRC患者。所有患者分为两个亚组:转移性CRC和非转移性CRC。最初,使用传统组织学技术检查肿瘤样本,然后用针对CD133和CD44标志物的单克隆抗体进行免疫组化分析。
在71.4%的转移性疾病患者中观察到CD133和CD44的高共表达,而在无远处转移的患者中这一比例为37.9%。在转移性CRC亚组的8%和无转移性CRC亚组的13.4%中发现了两种标志物的不一致表达。统计分析表明,CD133和CD44表达增加与疾病分期、T类别和N淋巴结状态显著相关。通过多元回归分析,疾病分期被确定为对CD133(p<0.0001)和CD44(p<0.0001)表达影响最大且具有统计学意义的因素。
CD133和CD44的共表达在预测CRC的转移形式中起重要作用。这两种干细胞标志物均可应用于标准病理组织学诊断,并且可能是治疗前肿瘤学筛查的有用标志物。